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Mariko Yagi

Showing results (51-60 of 76) with videos related to

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Molecular Vision|December 15, 2010
Molecular characterization of the 5'-UTR of retinal dystrophin reveals a cryptic intron that regulates translational activityIkuko Kubokawa, Yasuhiro Takeshima, Mitsunori Ota, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 23, 2013
A prostaglandin D2 metabolite is elevated in the urine of Duchenne muscular dystrophy patients and increases further from 8 years oldTaku Nakagawa, Atsuko Takeuchi, Ryohei Kakiuchi, et al.
Pediatric Research|April 22, 2006
Intravenous infusion of an antisense oligonucleotide results in exon skipping in muscle dystrophin mRNA of Duchenne muscular dystrophyYasuhiro Takeshima, Mariko Yagi, Hiroko Wada, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 12, 2010
Effect of CPS14217C>A genotype on valproic-acid-induced hyperammonemiaMariko Yagi, Tsutomu Nakamura, Yo Okizuka, et al.
Journal of Human Genetics|May 30, 2014
A novel splicing silencer generated by DMD exon 45 deletion junction could explain upstream exon 44 skipping that modifies dystrophinopathyEry Kus Dwianingsih, Rusdy Ghazali Malueka, Atsushi Nishida, et al.
BMC Genetics|April 3, 2012
Categorization of 77 dystrophin exons into 5 groups by a decision tree using indexes of splicing regulatory factors as decision markersRusdy Ghazali Malueka, Yutaka Takaoka, Mariko Yagi, et al.
Brain & Development|August 31, 2023
Improvement in a post-stroke pediatric patient with hemiplegia: Use of a hand-arm bimanual intensive therapy with hybrid assistive limbYoko Matsumoto, Yuji Yoshii, Akiyo Ikutomo, et al.
Journal of Human Genetics|December 21, 2006
Genetic polymorphisms associated with adverse events and elimination of methotrexate in childhood acute lymphoblastic leukemia and malignant lymphomaHiroyuki Imanishi, Noboru Okamura, Mariko Yagi, et al.
Molecular Genetics and Metabolism|July 20, 2010
A Japanese child with asymptomatic elevation of serum creatine kinase shows PTRF-CAVIN mutation matching with congenital generalized lipodystrophy type 4Ery Kus Dwianingsih, Yasuhiro Takeshima, Kyoko Itoh, et al.
Human Genetics|March 11, 2006
Co-occurrence of mutations in both dystrophin- and androgen-receptor genes is a novel cause of female Duchenne muscular dystrophyYoshinori Katayama, Van Khanh Tran, Nguyen Thi Hoan, et al.
Pageof 8

Showing results (51-60 of 76) with videos related to

Sort By:
Pageof 8
Molecular Vision|December 15, 2010
Molecular characterization of the 5'-UTR of retinal dystrophin reveals a cryptic intron that regulates translational activityIkuko Kubokawa, Yasuhiro Takeshima, Mitsunori Ota, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 23, 2013
A prostaglandin D2 metabolite is elevated in the urine of Duchenne muscular dystrophy patients and increases further from 8 years oldTaku Nakagawa, Atsuko Takeuchi, Ryohei Kakiuchi, et al.
Pediatric Research|April 22, 2006
Intravenous infusion of an antisense oligonucleotide results in exon skipping in muscle dystrophin mRNA of Duchenne muscular dystrophyYasuhiro Takeshima, Mariko Yagi, Hiroko Wada, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 12, 2010
Effect of CPS14217C>A genotype on valproic-acid-induced hyperammonemiaMariko Yagi, Tsutomu Nakamura, Yo Okizuka, et al.
Journal of Human Genetics|May 30, 2014
A novel splicing silencer generated by DMD exon 45 deletion junction could explain upstream exon 44 skipping that modifies dystrophinopathyEry Kus Dwianingsih, Rusdy Ghazali Malueka, Atsushi Nishida, et al.
BMC Genetics|April 3, 2012
Categorization of 77 dystrophin exons into 5 groups by a decision tree using indexes of splicing regulatory factors as decision markersRusdy Ghazali Malueka, Yutaka Takaoka, Mariko Yagi, et al.
Brain & Development|August 31, 2023
Improvement in a post-stroke pediatric patient with hemiplegia: Use of a hand-arm bimanual intensive therapy with hybrid assistive limbYoko Matsumoto, Yuji Yoshii, Akiyo Ikutomo, et al.
Journal of Human Genetics|December 21, 2006
Genetic polymorphisms associated with adverse events and elimination of methotrexate in childhood acute lymphoblastic leukemia and malignant lymphomaHiroyuki Imanishi, Noboru Okamura, Mariko Yagi, et al.
Molecular Genetics and Metabolism|July 20, 2010
A Japanese child with asymptomatic elevation of serum creatine kinase shows PTRF-CAVIN mutation matching with congenital generalized lipodystrophy type 4Ery Kus Dwianingsih, Yasuhiro Takeshima, Kyoko Itoh, et al.
Human Genetics|March 11, 2006
Co-occurrence of mutations in both dystrophin- and androgen-receptor genes is a novel cause of female Duchenne muscular dystrophyYoshinori Katayama, Van Khanh Tran, Nguyen Thi Hoan, et al.
Pageof 8